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MicroRNA-663 Regulates Melanoma Progression by Inhibiting FHL3.
Liu, Saijun; Hu, Yunfeng; Wu, Shi; He, Yong; Deng, Liehua.
Afiliação
  • Liu S; Department of Dermatology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Hu Y; Department of Dermatology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Wu S; Department of Dermatology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • He Y; Department of Dermatology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
  • Deng L; Department of Dermatology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Technol Cancer Res Treat ; 19: 1533033820957000, 2020.
Article em En | MEDLINE | ID: mdl-33000682
ABSTRACT
microRNA-663a (miR-663a) was reported to be highly expressed in cancers. However, its roles in melanoma progression remain unclear. Reverse transcription quantitative polymerase chain reaction (RT-qPCR) was conducted to measure miR-663a expression level in melanoma cell lines and normal cells. Cell counting kit-8 assay, wound-healing assay, and transwell invasion assay were conducted to analyze biological roles of miR-663a in melanoma. Luciferase activity reporter assay was conducted to validate the connection of miR-663a and Four and a half LIM domain (FHL) protein 3 (FHL3) in melanoma. Our results showed miR-663a expression level was significantly increased in melanoma cells compared with normal cells. Silencing miR-663a expression suppresses melanoma cell proliferation, migration, and invasion in vitro. Moreover, FHL3 was validated as a functional target of miR-663a. Knockdown of FHL3 partially rescued the inhibitory effects of miR-663a inhibitor on melanoma cell behaviors. Together, our work provided evidence that miR-663a functions as an oncogenic miRNA in melanoma.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Technol Cancer Res Treat Assunto da revista: NEOPLASIAS / TERAPEUTICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Technol Cancer Res Treat Assunto da revista: NEOPLASIAS / TERAPEUTICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China